rs876659900

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs876659900(C;T)

Make rs876659900(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

5982861

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs876659900
dbSNP (classic)	rs876659900
ClinGen	rs876659900
ebi	rs876659900
HLI	rs876659900
Exac	rs876659900
Gnomad	rs876659900
Varsome	rs876659900
LitVar	rs876659900
Map	rs876659900
PheGenI	rs876659900
Biobank	rs876659900
1000 genomes	rs876659900
hgdp	rs876659900
ensembl	rs876659900
geneview	rs876659900
scholar	rs876659900
google	rs876659900
pharmgkb	rs876659900
gwascentral	rs876659900
openSNP	rs876659900
23andMe	rs876659900
SNPshot	rs876659900
SNPdbe	rs876659900
MSV3d	rs876659900
GWAS Ctlg	rs876659900

Max Magnitude

0

ClinVar
Risk	rs876659900(T;T)
Alt	rs876659900(T;T)
Reference	Rs876659900(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PMS2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000007.13:g.6022492G>A
CLNSRC
CLNACC	RCV000216032.1,